TY - JOUR
T1 - Mechanically Robust, Forgeable, and Machinable Cellulose Hydrogel
AU - Liu, Xiaodi
AU - Tian, Yichen
AU - Kang, Shuhua
AU - Jin, Zhiping
AU - Chen, Lei
AU - Lu, Qiang
AU - Wang, Li
AU - Zhang, Qiang
N1 - Publisher Copyright:
© 2026 American Chemical Society
PY - 2026/2/2
Y1 - 2026/2/2
N2 - Tough hydrogels show great promise for flexible electronics, soft robotics, and biomedical applications, but their poor secondary formability limits their practical utility. Here, we developed a one-step regeneration–cross-linking strategy that simultaneously induced regeneration and ionic cross-linking of carboxymethyl cellulose through multivalent metal ions in acidic coagulation baths, producing tough, processable hydrogels. This method overcame key limitations of conventional two-step approaches, including uneven ion diffusion and cross-linking heterogeneity, enabling the fabrication of thick and bulk samples. The resulting Fe3+-cross-linked regenerated cellulose hydrogel (RCH-Fe) exhibited a uniform, dense network of sacrificial bonds, delivering exceptional energy dissipation and crack resistance. The optimized RCH-Fe achieved a compressive modulus of ∼9.4 MPa at ∼77.2% strain, while under tension it exhibited a Young’s modulus of ∼16.4 MPa with a strain of ∼61.4%. RCH-Fe maintained its structural integrity during secondary processing (forging/carving). Remarkably, dried RCH-Fe gains enhanced mechanical robustness, enabling jade-like precision sculpting, and demonstrates selective UV-blocking capabilities for optical applications. This work advances tough hydrogels toward high-end customized manufacturing.
AB - Tough hydrogels show great promise for flexible electronics, soft robotics, and biomedical applications, but their poor secondary formability limits their practical utility. Here, we developed a one-step regeneration–cross-linking strategy that simultaneously induced regeneration and ionic cross-linking of carboxymethyl cellulose through multivalent metal ions in acidic coagulation baths, producing tough, processable hydrogels. This method overcame key limitations of conventional two-step approaches, including uneven ion diffusion and cross-linking heterogeneity, enabling the fabrication of thick and bulk samples. The resulting Fe3+-cross-linked regenerated cellulose hydrogel (RCH-Fe) exhibited a uniform, dense network of sacrificial bonds, delivering exceptional energy dissipation and crack resistance. The optimized RCH-Fe achieved a compressive modulus of ∼9.4 MPa at ∼77.2% strain, while under tension it exhibited a Young’s modulus of ∼16.4 MPa with a strain of ∼61.4%. RCH-Fe maintained its structural integrity during secondary processing (forging/carving). Remarkably, dried RCH-Fe gains enhanced mechanical robustness, enabling jade-like precision sculpting, and demonstrates selective UV-blocking capabilities for optical applications. This work advances tough hydrogels toward high-end customized manufacturing.
KW - deformation
KW - high strength and toughness
KW - ion-cross-linking
KW - one-step synthesis
KW - regenerated cellulose hydrogel
UR - https://www.scopus.com/pages/publications/105029903531
U2 - 10.1021/acssuschemeng.5c13794
DO - 10.1021/acssuschemeng.5c13794
M3 - 文章
AN - SCOPUS:105029903531
SN - 2168-0485
VL - 14
SP - 2256
EP - 2265
JO - ACS Sustainable Chemistry and Engineering
JF - ACS Sustainable Chemistry and Engineering
IS - 4
ER -